510(k) K901548
K901548 is an FDA 510(k) premarket notification submitted by Shiley, Inc. for the device "BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GAS". The FDA issued a decision of Substantially Equivalent on January 14, 1991. The device falls under product code CCC (Analyzer, Gas, Carbon-Dioxide, Partial Pressure, Blood-Phase, Indwelling), a Class II device regulated under 21 CFR 868.1150. Shiley, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 1991
- Date Received
- April 3, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Analyzer, Gas, Carbon-Dioxide, Partial Pressure, Blood-Phase, Indwelling
- Device Class
- Class II
- Regulation Number
- 868.1150
- Review Panel
- AN
- Submission Type